EP0023607A2 - Process for preparing a collagen solution, such a solution and its use - Google Patents

Process for preparing a collagen solution, such a solution and its use Download PDF

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Publication number
EP0023607A2
EP0023607A2 EP80103996A EP80103996A EP0023607A2 EP 0023607 A2 EP0023607 A2 EP 0023607A2 EP 80103996 A EP80103996 A EP 80103996A EP 80103996 A EP80103996 A EP 80103996A EP 0023607 A2 EP0023607 A2 EP 0023607A2
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EP
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Prior art keywords
collagen
solution
viii
plasma
collagen solution
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EP80103996A
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German (de)
French (fr)
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EP0023607A3 (en
EP0023607B1 (en
Inventor
Udo Dr. Becker
Konrad Braun
Norbert Dr. Heimburger
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Siemens Healthcare Diagnostics GmbH Germany
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Behringwerke AG
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    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/10—Transferases (2.)
    • C12N9/1025—Acyltransferases (2.3)
    • C12N9/104—Aminoacyltransferases (2.3.2)
    • C12N9/1044—Protein-glutamine gamma-glutamyltransferase (2.3.2.13), i.e. transglutaminase or factor XIII
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/64—Proteins; Peptides; Derivatives or degradation products thereof
    • A61K8/65—Collagen; Gelatin; Keratin; Derivatives or degradation products thereof
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
    • A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
    • A61L15/22—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing macromolecular materials
    • A61L15/32—Proteins, polypeptides; Degradation products or derivatives thereof, e.g. albumin, collagen, fibrin, gelatin
    • A61L15/325—Collagen
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
    • A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
    • A61L15/42—Use of materials characterised by their function or physical properties
    • A61L15/425—Porous materials, e.g. foams or sponges
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L26/00—Chemical aspects of, or use of materials for, wound dressings or bandages in liquid, gel or powder form
    • A61L26/0009—Chemical aspects of, or use of materials for, wound dressings or bandages in liquid, gel or powder form containing macromolecular materials
    • A61L26/0028—Polypeptides; Proteins; Degradation products thereof
    • A61L26/0033—Collagen
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A61P7/04—Antihaemorrhagics; Procoagulants; Haemostatic agents; Antifibrinolytic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00—Preparations for care of the skin
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/745—Blood coagulation or fibrinolysis factors
    • C07K14/755—Factors VIII, e.g. factor VIII C (AHF), factor VIII Ag (VWF)
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/78—Connective tissue peptides, e.g. collagen, elastin, laminin, fibronectin, vitronectin, cold insoluble globulin [CIG]
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/86—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving blood coagulating time or factors, or their receptors
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2333/00—Assays involving biological materials from specific organisms or of a specific nature
    • G01N2333/435—Assays involving biological materials from specific organisms or of a specific nature from animals; from humans
    • G01N2333/745—Assays involving non-enzymic blood coagulation factors
    • G01N2333/755—Factors VIII, e.g. factor VIII C [AHF], factor VIII Ag [VWF]
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2333/00—Assays involving biological materials from specific organisms or of a specific nature
    • G01N2333/435—Assays involving biological materials from specific organisms or of a specific nature from animals; from humans
    • G01N2333/78—Connective tissue peptides, e.g. collagen, elastin, laminin, fibronectin, vitronectin, cold insoluble globulin [CIG]
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2333/00—Assays involving biological materials from specific organisms or of a specific nature
    • G01N2333/90—Enzymes; Proenzymes
    • G01N2333/91—Transferases (2.)
    • G01N2333/91045—Acyltransferases (2.3)
    • G01N2333/91074—Aminoacyltransferases (general) (2.3.2)
    • G01N2333/9108—Aminoacyltransferases (general) (2.3.2) with definite EC number (2.3.2.-)
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2333/00—Assays involving biological materials from specific organisms or of a specific nature
    • G01N2333/90—Enzymes; Proenzymes
    • G01N2333/91—Transferases (2.)
    • G01N2333/91045—Acyltransferases (2.3)
    • G01N2333/91074—Aminoacyltransferases (general) (2.3.2)
    • G01N2333/9108—Aminoacyltransferases (general) (2.3.2) with definite EC number (2.3.2.-)
    • G01N2333/91085—Transglutaminases; Factor XIIIq (2.3.2.13)

Definitions

  • the invention relates to a method for producing a collagen solution from human or animal tissue, especially from human umbilical cord and placenta, and its use for the adsorption of coagulation factors VIII and XIII.
  • the invention relates to a process for the production of collagen, characterized in that pepsin-treated collagen against a buffer solution of pH 7-8.5, preferably a phosphate-buffered isotonic salt solution of pH 7.2, which contains a basic amino acid, preferably arginine, in a concentration of 5-20, preferably 10 nmol / 1, dialyzed.
  • a buffer solution of pH 7-8.5 preferably a phosphate-buffered isotonic salt solution of pH 7.2, which contains a basic amino acid, preferably arginine, in a concentration of 5-20, preferably 10 nmol / 1, dialyzed.
  • a suitable pepsin-treated collagen can be obtained, for example, by using human or animal tissue, preferably human umbilical cord or placenta, with a suitable buffer solution of pH 7-9, which may contain neutral salts, preferably with a Tris-hydrochloric acid buffer of pH 7.4 Sodium chloride and optionally a complexing agent, for example EDTA, citrate or phosphate, preferably EDTA and / or a proteinase inhibitor, for example soybean trypsin or Kunitzinhibitor or preferably aprotinin, extracted, the separated precipitate extracted with the same buffer solution, which, however, no complexing agent and contains no inhibitor, the separated precipitate is treated with an aqueous solution of an acid with a pK of 3-5, preferably with 0.5 molar acetic acid, the separated precipitate in an aqueous solution of an acid with a pK of 3-5, preferably with 0.1 molar acetic acid, absorbs, pref possibly brought to pH 2 with hydroch
  • a collagen solution obtained in this way secretes collagen fibrils when it is heated to at least about 37 ° C. If the solution is heated in the presence of coagulation factors VIII and XIII, the precipitated fibrils adsorb these factors in an active form. The temperature is chosen so that a high yield of active factors is obtained. This property can serve to further identify the collagen that can be obtained by the method according to the invention, the individual process measures of which are known in part.
  • the invention is important for the production of concentrates of factor VIII and XIII, which are used for the therapy of certain coagulation and wound healing disorders.
  • the treatment of hemophilia A with the factor VIII concentrates available today is expensive, since only about 10% of the factor VIII content present in the plsma is obtained during its production. A process with better yield is therefore of interest.
  • the collagen preparation produced according to the invention is furthermore suitable for the manufacture of wound coverings which are suitable for hemostasis, especially also in patients with a particular tendency to bleed (hemophilia), for example after tooth extractions.
  • human plasma is adsorbed on the collagen preparation, unbound plasma parts are washed out and lyophilized.
  • the fleece-like collagen obtained in this way contains all the components necessary for hemostasis, fibrin stabilization and wound healing.
  • the collagen preparation to which the coagulation factors are adsorbed can be used as a diagnostic agent to detect platelet function disorders. If, for example, blood or a platelet-rich plasma supernatant from healthy people is mixed with a collagen solution prepared according to the invention at a temperature at which fibrils can form, the platelets clump. In certain pathological conditions, there is no response. The spontaneous formation of fibrils makes the collagen solution particularly suitable as a diagnostic agent. The suspensions used so far cannot be standardized with regard to the size of the fibrils.
  • Such a collagen solution or col. Layer suspension is also suitable for use for cosmetic purposes, particularly since it is homologous collagen.
  • the precipitate is suspended in 0.5 l of extraction buffer II, which corresponds to extraction buffer I but does not contain any antagosan (R) , and centrifuged again after 30 min. Now the precipitate is suspended in 0.5 1 0.5 molar acetic acid and zen after 30 min centrifuged. The precipitate is taken up in 2 liters of fresh 0.5 molar acetic acid and stirred at 4 ° C. for 24 hours. After centrifugation and discarding of the supernatant, the precipitate is taken up in 3 1 0.1 molar acetic acid and brought to pH 2 with stirring with 1 N hydrochloric acid under pH control.
  • extraction buffer II which corresponds to extraction buffer I but does not contain any antagosan (R)
  • pepsin from Serva, 30 Anson units per mg
  • pepsin from Serva, 30 Anson units per mg
  • the mixture is stirred at a temperature of 25 ° C. for 24 hours. It is centrifuged, the supernatant is saved and the residue, mixed with fresh pepsin, is broken down again under the same conditions. Under the conditions mentioned, the umbilical cord tissue is completely dissolved. Both extracts are combined and brought to a concentration of 0.9 mol / 1 with solid NaCl. After stirring for 2 hours, the mixture is centrifuged and the supernatant is discarded. The precipitate is dissolved in 3 1 0.05 M Tris / HCl, pH 7.4, containing 1 mol / 1 NaCl.
  • 1 1 of this solution is against 2 times 5 1 phosphate-buffered physiological sodium chloride pH 7.2 (8 g / 1 sodium chloride, 1.15 g / l disodium hydrogen phosphate, 0.2 g / 1 potassium dihydrogen phosphate) containing 0.01 mol / 1 arginine dialysed for 24 hours at room temperature and then a concentration of 1 mg collagen per ml was set with the dialysis buffer.
  • Example 2 The experiment described in Example 2 is carried out with human blood plasma containing 4 IU heparin / ml as an anticoagulant.
  • the results for F VIII R: AG and F VIII R: WF correspond to those of Example 2.
  • F VIII: C cannot be determined in a heparin-containing environment for methodological reasons.
  • the precipitate of collagen fibrils produced according to Example 1 with the addition of 1 mg collagen / ml plasma is washed three times with 1 ml of physiological saline and suspended in a concentration of 5 mg / ml in physiological saline.
  • Tube 1 receives 0.1 ml of a plasma prediluted 1: 5 in normal saline with normal factor VIII content.
  • Tube 2 receives 0.1 ml of the plasma-loaded and washed collagen fibrils.
  • Tube 3 receives 0.1 ml of the unloaded adsorbed collagen fibrils.
  • Tube 4 receives 0.1 ml of physiological saline.
  • a kaolin platelet factor 3 mixture (Pathromtin (R) from Behringwerke AG, Marburg) is added to each tube. After mixing, six minutes. Incubated at 37 ° C, then 0.1 ml of a 0.025 molar calcium chloride solution was added to each tube and the clotting times determined. The result is shown in Table 1.
  • the coagulation times show that a collagen suspension prepared according to the invention and adsorbed with normal plasma contains biologically active coagulation factor VIII.
  • 1 ml of collagen solution is loaded as in Example 2 with 1 ml of citrate-containing human plasma, the collagen fibrils are centrifuged off and washed three times with phosphate-buffered physiological saline. The collagen fibrils are examined with rabbit antisera specific for certain plasma proteins in an indirect fluorescence test for adsorbed plasma proteins. A negative reaction is found with normal rabbit serum and a very weak reaction with anti-human fibrinogen, anti-human immunoglobulin and anti-human albumin. A very strong reaction is found with anti-human factor VIII serum.
  • This example shows the selective and specific binding of factor VIII, which is, for example, contained in the plasma at 4,400 times lower concentration than albumin.
  • Example 5 is carried out with the plasma of a patient with von Willbrand's disease, whose factor VIII content is less than 10% of the norm. A weak response is observed with factor VIII antiserum.
  • human citrate plasma is adsorbed with increasing amounts of collagen.
  • the plasma supernatants are examined for their content of factor XIII.
  • the test used is a qualitative procedure that gives the activity ranges in% based on normal plasma. Taking into account the initial dilution of 1: 2, the% values given in Table 2 are found.
  • the collagen solution is heated to about 35 to 40 ° C so that it excretes fibrils.
  • the gel-like mass is lyophilized, whereby a stable white collagen fleece is obtained.
  • Factor VIII, Factor XIII and / or fibrinogen may have been added to the collagen solution.

Abstract

Process for the manufacture of a collagen solution and its use for the manufacture of collagen fibrillae for adsorbing coagulation factors, as diagnostic agent, for the manufacture of a collagen sponge and for use in a cosmetic preparation.

Description

Die Erfindung betrifft ein Verfahren zur Herstellung einer Kollagenlösung aus menschlichem oder tierischem Gewebe, vor allem aus menschlicher Nabelschnur und Plazenta, und dessen Verwendung zur Adsorption der Gerinnungsfaktoren VIII und XIII.The invention relates to a method for producing a collagen solution from human or animal tissue, especially from human umbilical cord and placenta, and its use for the adsorption of coagulation factors VIII and XIII.

Verfahren zur Herstellung von Kollagen sind bekannt. Es ist auch bekannt, daß eine bestimmte Kollagen-Präparation das Faktor VIII-Antigen zu binden vermag, während die Faktor VIII-Aktivität im Überstand bleibt (Nyman, D., Thrombos.Research 11, (1977), 433).Methods for producing collagen are known. It is also known that a particular collagen preparation can bind the factor VIII antigen while the factor VIII activity remains in the supernatant (Nyman, D., Thrombos. Research 11, (1977), 433).

Die bisher beschriebenen Präparate sind für die Gewinnung der genannten Faktoren über ihre selektive und quantitative Adsorption, beispielsweise aus Blutplasma, nicht brauchbar. An einem derartigen Kollagen besteht jedoch wegen der Bedeutung und dem Bedarf an diesen Faktoren für die Behandlung von Gerinnungs- und Wundheilungsstörungen Interesse, insbesondere auch zur Verwendung als Grundmaterial für die Herstellung von Vliesen.The preparations described hitherto cannot be used to obtain the factors mentioned via their selective and quantitative adsorption, for example from blood plasma. However, because of the importance and the need for these factors for the treatment of coagulation and wound healing disorders, there is interest in such a collagen, in particular also for use as a base material for the production of nonwovens.

Es wurde nun überraschenderweise gefunden, daß ein unter bestimmten Bedingungen hergestelltes Kollagen die Gerinnungsfaktoren VIII und XIII zu adsorbieren vermag.It has now surprisingly been found that a collagen produced under certain conditions can adsorb coagulation factors VIII and XIII.

Gegenstand der Erfindung ist ein Verfahren zur Herstellung von Kollagen, dadurch gekennzeichnet, daß pepsinbehandeltes Kollagen gegen eine Pufferlösung von pH 7-8,5, vorzugsweise eine phosphatgepufferte isotonische Salzlösung von pH 7,2, die eine basische Aminosäure, vorzugsweise Arginin, in einer Konzentration von 5 - 20, vorzugsweise 10 nmol/1 enthält, dialysiert wird.The invention relates to a process for the production of collagen, characterized in that pepsin-treated collagen against a buffer solution of pH 7-8.5, preferably a phosphate-buffered isotonic salt solution of pH 7.2, which contains a basic amino acid, preferably arginine, in a concentration of 5-20, preferably 10 nmol / 1, dialyzed.

Ein geeignetes pepsinbehandeltes Kollagen kann beispielsweise dadurch erhalten werden, daß man menschliches oder tierisches Gewebe vorzugsweise menschliche Nabelschnur oder Plazenten, mit einer geeigneten Pufferlösung von pH 7-9, die Neutralsalze enthalten kann, vorzugsweise mit einem Tris-Salzsäurepuffer von pH 7,4, der Natriumchlorid und gegebenenfalls einen Komplexbildner, beispielsweise EDTA, Citrat oder Phosphat, vorzugsweise EDTA und/oder einen Proteinaseninhibitor, beispielsweise Soja-Trypsin- oder Kunitzinhibitor oder vorzugsweise Aprotinin, enthält, extrahiert, den abgetrennten Niederschlag mit der gleichen Pufferlösung extrahiert, die jedoch keinen Komplexbildner und keinen Inhibitor enthält, den abgetrennten Niederschlag mit einer wässrigen Lösung einer Säure mit einem pK von 3-5, vorzugsweise mit 0,5 molarer Essigsäure, behandelt, den abgetrennten Niederschlag in einer wässrigen Lösung einer Säure mit einem pK von 3-5, vorzugsweise mit 0,1 molarer Essigsäure, aufnimmt, vorzugsweise mit Salzsäure auf pH 2 bringt, mit Pepsin, vorzugsweise einen Tag bei 4 - 25°C, vorzugsweise 25°C, behandelt, den Überstand abtrennt, die Pepsinbehandlung am Rückstand wiederholt, den Überstand abtrennt, die beiden Überstände vereinigt, durch Erhöhen der Ionenstärke durch Zugabe von Neutralsalz auf 1 - 1,3 mol/1 das Kollagen ausfällt, den abgetrennten Niederschlag in einer Pufferlösung von pH 7 - 8,5, vorzugsweise einem Tris-Salzsäurepuffer von pH 7,4, der Neutralsalz enthält, löst, gegen den gleichen Puffer dialysiert, gegebenenfalls die Lösung mit einem silikathaltigen Adsorptionsmittel, wie Kaolin, Aerosil, beispielsweise mit Decalite speedplus (Degussa, Frankfurt, Bundesrepublik Deutschland) versetzt und die Kollagen-Lösung abtrennt.A suitable pepsin-treated collagen can be obtained, for example, by using human or animal tissue, preferably human umbilical cord or placenta, with a suitable buffer solution of pH 7-9, which may contain neutral salts, preferably with a Tris-hydrochloric acid buffer of pH 7.4 Sodium chloride and optionally a complexing agent, for example EDTA, citrate or phosphate, preferably EDTA and / or a proteinase inhibitor, for example soybean trypsin or Kunitzinhibitor or preferably aprotinin, extracted, the separated precipitate extracted with the same buffer solution, which, however, no complexing agent and contains no inhibitor, the separated precipitate is treated with an aqueous solution of an acid with a pK of 3-5, preferably with 0.5 molar acetic acid, the separated precipitate in an aqueous solution of an acid with a pK of 3-5, preferably with 0.1 molar acetic acid, absorbs, pref possibly brought to pH 2 with hydrochloric acid, treated with pepsin, preferably for one day at 4-25 ° C., preferably 25 ° C., the supernatant separated, the pepsin treatment repeated on the residue, the supernatant separated, the two supernatants combined, by increasing the Ionic strength by adding neutral salt to 1 - 1.3 mol / 1 the collagen precipitates, dissolves the separated precipitate in a buffer solution of pH 7-8.5, preferably a tris-hydrochloric acid buffer of pH 7.4, which contains neutral salt dialyzed the same buffer, if necessary the solution with a silicate-containing adsorbent such as kaolin, Aerosil, for example with Decalite speedplus (Degussa, Frankfurt, Federal Republic of Germany) and the collagen solution is separated.

Eine auf diese Weise erhaltene Kollagenlösung scheidet Kollagenfibrillen aus, wenn sie auf mindestens etwa 370C erwärmt wird. Wird die Lösung in Gegenwart der Gerinnungsfaktoren VIII und XIII erwärmt, adsorbieren die ausfallenden Fibrillen diese Faktoren in aktiver Form. Die Temperatur wird so gewählt, daß man eine hohe Ausbeute an aktiven Faktoren erhält. Diese Eigenschaft kann zur weiteren Kennzeichnung des Kollagens dienen, das nach dem erfindungsgemäßen Verfahren erhalten werden kann, dessen einzelne Verfahrensmaßnahmen zum Teil bekannt sind.A collagen solution obtained in this way secretes collagen fibrils when it is heated to at least about 37 ° C. If the solution is heated in the presence of coagulation factors VIII and XIII, the precipitated fibrils adsorb these factors in an active form. The temperature is chosen so that a high yield of active factors is obtained. This property can serve to further identify the collagen that can be obtained by the method according to the invention, the individual process measures of which are known in part.

Die Erfindung ist für die Herstellung von Konzentraten von Faktor VIII und XIII von Bedeutung, die zur Therapie bestimmter Gerinnungs- und Wundhei,lungsstörungen eingesetzt werden. Die Therapie der Hämophilie A ist mit den heute verfügbaren Faktor VIII-Konzentraten teuer, da bei ihrer Herstellung nur etwa 10 % des im Plsma vorhandenen Gehalts an Faktor VIII erhalten werden. Ein Verfahren mit besserer Ausbeute ist daher von Interesse.The invention is important for the production of concentrates of factor VIII and XIII, which are used for the therapy of certain coagulation and wound healing disorders. The treatment of hemophilia A with the factor VIII concentrates available today is expensive, since only about 10% of the factor VIII content present in the plsma is obtained during its production. A process with better yield is therefore of interest.

Das erfindungsgemäß hergestellte Kollagenpräparat eignet sich weiterhin für die Herstellung von Wundabdeckungen, die zur Blutstillung, speziell auch bei Patienten mit besonderer Blutungsneigung (Hämophilie), beispielsweise nach Zahnextraktionen, geeignet sind. Hierfür wird menschliches Plasma an das Kollagenpräparat adsorbiert, nicht gebundene Plasmateile ausgewaschen und lyophilisiert. Das so gewonnene vliesartige Kollagen enthält alle für die Blutstillung, Fibrinstabilisierung und Wundheilung notwendigen Bestandteile.The collagen preparation produced according to the invention is furthermore suitable for the manufacture of wound coverings which are suitable for hemostasis, especially also in patients with a particular tendency to bleed (hemophilia), for example after tooth extractions. For this purpose, human plasma is adsorbed on the collagen preparation, unbound plasma parts are washed out and lyophilized. The fleece-like collagen obtained in this way contains all the components necessary for hemostasis, fibrin stabilization and wound healing.

Außerdem kann das Kollagenpräparat, an das die Gerinnungsfaktoren adsorbiert sind, verwendet, werden als Diagnostikum, um Störungen der Thrombozytenfunktion zu erkennen. Mischt man beispielsweise Blut oder einen Thrombozyten-reichen Plasmaüberstand gesunder Personen mit einer erfindungsgemäß hergestellten Kollagenlösung bei einer Temperatur, bei der Fibrillen entstehen können, verklumpen die Thrombozyten. Bei bestimmten pathologischen Zuständen bleibt die Reaktion aus. Die spontane Fibrillenbildung macht die Kollagenlösung besonders gut als Diagnostikum geeignet. Die bisher verwendeten Suspensionen sind bezüglich der Fibrillengröße nicht standardisierbar.In addition, the collagen preparation to which the coagulation factors are adsorbed can be used as a diagnostic agent to detect platelet function disorders. If, for example, blood or a platelet-rich plasma supernatant from healthy people is mixed with a collagen solution prepared according to the invention at a temperature at which fibrils can form, the platelets clump. In certain pathological conditions, there is no response. The spontaneous formation of fibrils makes the collagen solution particularly suitable as a diagnostic agent. The suspensions used so far cannot be standardized with regard to the size of the fibrils.

Eine solche Kollagenlösung oder Kol.lagensuspension ist auch zur Verwendung für kosmetische Zwecke geeignet, besonders, da es sich um homologes Kollagen handelt.Such a collagen solution or col. Layer suspension is also suitable for use for cosmetic purposes, particularly since it is homologous collagen.

Testmethoden:Test methods:

Bestimmung des Gerinnungsfaktors VIII :

  • F VIII:C : Mit der Faktor VIII-Einphasen-Bestimmung mit dem Testkit der Behringwerke AG,Marburg,Bundesrepublik Deutschland
  • F VIII R:AG: Immunologisch nach LAURELL, C.-B., Anal. Biochem. 10, 358 (1965)
  • F VIII R:WF: Funktionell mit Ristocetin nach H.-J. WEISS et al., J.Clin.Invest.52, 2708 (1973)
  • F XIII : Mit der Faktor XIII-Einphasen-Bestimnung mit dem Schnelltest d.Behringwerke AG,Marburg,Bundesrepublik Deutschland
  • Blutplättchenaggregation: Nach BORN, G.W.R., J.Physiol. (London) 162, 67 (1962)
  • Immunfluoreszenz: Nach WICK, G., BAUDNER, F. und HERZOG, F.: Immunfluoereszenz, Med.Verlagsgesellschaft Marburg 1976
  • Hydroxyprolinbestimmung: Nach WOESSNER, J.F., Arch. Biochem.Biophys. 95, 440 (1961)
Determination of coagulation factor VIII:
  • F VIII: C: With the factor VIII single-phase determination with the test kit from Behringwerke AG, Marburg, Federal Republic of Germany
  • F VIII R: AG: Immunologically according to LAURELL, C.-B., Anal. Biochem. 10, 358 (1965)
  • F VIII R: WF: Functional with ristocetin according to H.-J. WEISS et al., J.Clin.Invest. 52, 2708 (1973)
  • F XIII: With the factor XIII single-phase determination with the rapid test of B.Behringwerke AG, Marburg, Federal Republic of Germany
  • Platelet aggregation: According to BORN, GWR, J. Physiol. (London) 162, 67 (1962)
  • Immunofluorescence: According to WICK, G., BAUDNER, F. and HERZOG, F .: Immunofluorescence, Med.Verlagsgesellschaft Marburg 1976
  • Hydroxyproline determination: According to WOESSNER, JF, Arch. Biochem.Biophys. 95, 440 (1961)

Die Erfindung soll durch die nachstehenden Beispiele näher erläutert werden.The invention is illustrated by the examples below.

Beispiel 1: Herstellung des KollagensExample 1: Preparation of the collagen

10 tiefgefrorene Nabelschnüre werden aufgetaut und in 1 cm lange Stücke geschnitten. Die Stücke werden zusammen mit 0,5 1 Extraktionspuffer 1 (0,05 m Tris/HCL, pH 7,4, enthaltend 0,5 m NaCl, 0,01 m EDTA, 250 E/1 Antagosan(R)) mit einem Messerhomogenisator fein verteilt. Das Gemisch wird zentrifugiert und der Überstand verworfen. Der Niederschlag wird in 2 1 Extraktionspuffer 1 24 Stunden bei 4°C gerührt. Es wird zentrifugiert und der Überstand verworfen. Der Niederschlag wird in 0,5 1 Extraktionspuffer II, welcher dem Extraktionspuffer I entspricht, jedoch kein Antagosan (R) enthält, suspendiert und nach 30 min erneut zentrifugiert. Nun wird der Niederschlag in 0,5 1 0,5 molarer Essigsäure suspendiert und nach 30 min zentrifugiert. Der Niederschlag wird in 2 1 frischer 0,5 molarer Essigsäure aufgenommen und 24 Stunden bei 4°C gerührt. Nach Zentrifugation und Verwerfen des Überstandes wird der Niederschlag in 3 1 0,1 molarer Essigsäure aufgenommen und unter Rühren mit 1 n Salzsäure unter pH-Kontrolle auf einen pH-Wert von 2 gebracht. Es wird 0,5 g Pepsin (Fa. Serva, 30 Anson-Einheiten pro mg) zugegeben und 24 Stunden bei einer Temperatur von 25°C gerührt. Es wird zentrifugiert, der Überstand wird aufbewahrt und der Rückstand, mit frischem Pepsin versetzt, unter denselben Bedingungen erneut abgebaut. Unter den genannten Bedingungen erfolgt eine völlige Auflösung des Nabelschnurgewebes. Beide Extrakte werden vereinigt und mit festem NaC1 auf eine Konzentration von 0,9 mol/1 gebracht. Nach 2-stündigem Rühren wird zentrifugiert und der überstand verworfen. Das Präzipitat wird in 3 1 0,05 m Tris/HCI, pH 7,4, enthaltend 1 mol/1 NaCl gelöst. Nach Auflösung wird gegen denselben Puffer, je zweimal 10 1, für 48 Stunden dialysiert. Die Lösung wird mit 20 g/l Decalite speedplus vermischt und zentrifugiert. Die klare Lösung hat einen Kollagengehalt von 1,8 mg/ml.10 frozen umbilical cords are thawed and cut into 1 cm long pieces. The pieces are mixed with 0.5 l of extraction buffer 1 (0.05 m Tris / HCl, pH 7.4, containing 0.5 m NaCl, 0.01 m EDTA, 250 U / 1 Antagosan (R) ) with a knife homogenizer finely divided. The mixture is centrifuged and the supernatant discarded. The precipitate is stirred in 2 1 extraction buffer 1 for 24 hours at 4 ° C. It is centrifuged and the supernatant is discarded. The precipitate is suspended in 0.5 l of extraction buffer II, which corresponds to extraction buffer I but does not contain any antagosan (R) , and centrifuged again after 30 min. Now the precipitate is suspended in 0.5 1 0.5 molar acetic acid and zen after 30 min centrifuged. The precipitate is taken up in 2 liters of fresh 0.5 molar acetic acid and stirred at 4 ° C. for 24 hours. After centrifugation and discarding of the supernatant, the precipitate is taken up in 3 1 0.1 molar acetic acid and brought to pH 2 with stirring with 1 N hydrochloric acid under pH control. 0.5 g of pepsin (from Serva, 30 Anson units per mg) is added and the mixture is stirred at a temperature of 25 ° C. for 24 hours. It is centrifuged, the supernatant is saved and the residue, mixed with fresh pepsin, is broken down again under the same conditions. Under the conditions mentioned, the umbilical cord tissue is completely dissolved. Both extracts are combined and brought to a concentration of 0.9 mol / 1 with solid NaCl. After stirring for 2 hours, the mixture is centrifuged and the supernatant is discarded. The precipitate is dissolved in 3 1 0.05 M Tris / HCl, pH 7.4, containing 1 mol / 1 NaCl. After dissolution, dialysis is carried out against the same buffer, twice 10 l, for 48 hours. The solution is mixed with 20 g / l Decalite speedplus and centrifuged. The clear solution has a collagen content of 1.8 mg / ml.

1 1 dieser Lösung wird gegen 2 mal 5 1 Phosphat-gepuffertes physiologisches Kochsalz pH 7,2 (8 g/1 Kochsalz, 1,15 g/l Di-natrium-hydrogenphosphat, 0,2 g/1 Kaliumdihydrogenphosphat) enthaltend 0,01 mol/1 Arginin 24 Stunden bei Raumtemperatur dialysiert und anschließend mit dem Dialysepuffer eine Konzentration von 1 mg Kollagen pro ml eingestellt.1 1 of this solution is against 2 times 5 1 phosphate-buffered physiological sodium chloride pH 7.2 (8 g / 1 sodium chloride, 1.15 g / l disodium hydrogen phosphate, 0.2 g / 1 potassium dihydrogen phosphate) containing 0.01 mol / 1 arginine dialysed for 24 hours at room temperature and then a concentration of 1 mg collagen per ml was set with the dialysis buffer.

Beispiel 2:Example 2:

5 mal 2 ml menschliches Blutplasma, enthaltend 10 Volunenteile 3,8 %ige Citratlösung als Anti koagulans, werden im Wasserbad auf 370C gebracht und mit steigenden Mengen der nach Beispiel 1 erhaltenen Kollagenlösung versetzt, wobei Volumenausgleich durch Phosphat-gepufferte Kochsalzlösung, pH 7,2, enthaltend 0,01 mol/1 Arginin, erfolgt. Die zugesetzten Mengen an Kollagen entsprechen 0, 1, 0,2, 0,5 und 1,0 mg/ml Plasma. Es wird 10 min bei 37°C inkubiert und dann 10 min bei 1.500 g zentrifugiert. Die Plasmaüberstände und die präzipitierten Kollagenfibrillen werden durch Abgießen voneinander getrennt. In den Plasmaüberständen wird die Faktor VIII-Aktivität bestimmt. Die Aktivitäten der drei biologischen Funktionen des Faktor VIII-Moleküls, Faktor VIII-Gerinnungsaktivität (F VIII:C), Faktor VIII-Antigen (F VIII R:AG) und v.Willebrand-Faktor (F VIII R:WF) werden im gleichen Maße bei der höchsten Kollagenkonzentration nahezu quantitativ aus der Lösung entfernt.5 times 2 ml of human blood plasma containing 10 Volunenteile 3.8% sodium citrate as anti-coagulant are placed in a water bath at 37 0 C, and treated with increasing amounts of the collagen solution obtained according to Example 1, wherein the volume compensating by phosphate-buffered saline, pH 7 , 2, containing 0.01 mol / 1 arginine. The added amounts of collagen correspond to 0, 1, 0.2, 0.5 and 1.0 mg / ml plasma. It is incubated at 37 ° C. for 10 min and then centrifuged at 1,500 g for 10 min. The plasma supernatants and the precipitated collagen fibrils are separated from one another by pouring. The factor VIII activity is determined in the plasma supernatants. The activities of the three biological functions of the factor VIII molecule, factor VIII coagulation activity (F VIII: C), factor VIII antigen (F VIII R: AG) and v.Willebrand factor (F VIII R: WF) are the same Measurements at the highest collagen concentration almost quantitatively removed from the solution.

Beispiel 3:Example 3:

Der in Beispiel 2 beschriebene Versuch wird mit menschlichem Blutplasma, enthaltend 4 IE Heparin/ml als Antikoagulans, durchgeführt. Die Ergebnisse für F VIII R:AG und F VIII R:WF entsprechen denen von Beispiel 2. F VIII:C kann in Heparin-haltigem Milieu aus methodischen Gründen nicht bestimmt werden.The experiment described in Example 2 is carried out with human blood plasma containing 4 IU heparin / ml as an anticoagulant. The results for F VIII R: AG and F VIII R: WF correspond to those of Example 2. F VIII: C cannot be determined in a heparin-containing environment for methodological reasons.

Beispiel 4:Example 4:

Das nach Beispiel 1 unter Zusatz von 1 mg Kollagen/ml Plasma hergestellte Präzipitat von Kollagenfibrillen wird dreimal mit je 1 ml physiologischer Kochsalzlösung gewaschen und in einer Konzentration von 5 mg/ml in physiologischer Kochsalzlösung suspendiert. Als Vergleichsprobe dient eine gleichermaßen gewaschene Kollagenfibrillensuspension gleicher Konzentration, die durch 10 minütiges Erwärmen eines entsprechenden Volumens der Kollagenlösung auf 37°C hergestellt wurde.The precipitate of collagen fibrils produced according to Example 1 with the addition of 1 mg collagen / ml plasma is washed three times with 1 ml of physiological saline and suspended in a concentration of 5 mg / ml in physiological saline. A similarly washed collagen fibril suspension of the same concentration, which was prepared by heating a corresponding volume of the collagen solution to 37 ° C. for 10 minutes, serves as a comparison sample.

In einem Gerinnungsautomaten nach Schnitger & Gross (Firma H.Amelung, 4922 Brake, Bundesrepublik Deutschland) werden vier Röhrchen mit je 0,1 ml eines kongenitalen Faktor VIII-Mangelplasmas vorgelegt und auf 370C erwärmt. Röhrchen 1 erhält 0,1 ml eines 1 : 5 in physiologischer Kochsalzlösung vorverdünnten Plasmas mit normalem Faktor VIII-Gehalt. Röhrchen 2 erhält 0,1 ml der mit Plasma beladenen und gewaschenen Kollagenfibrillen. Röhrchen 3 erhält 0,1 ml der nicht beladenen adsorbierten Kollagenfibrillen. Röhrchen 4 erhält 0,1 ml physiologische Kochsalzlösung.In a coagulation analyzer according to Schnitger & Gross (company H.Amelung, 4922 Brake, Federal Republic of Germany), four tubes with 0.1 ml of a congenital factor VIII-deficient plasma introduced and heated to 37 0 C. Tube 1 receives 0.1 ml of a plasma prediluted 1: 5 in normal saline with normal factor VIII content. Tube 2 receives 0.1 ml of the plasma-loaded and washed collagen fibrils. Tube 3 receives 0.1 ml of the unloaded adsorbed collagen fibrils. Tube 4 receives 0.1 ml of physiological saline.

Nun gibt man in jedes Röhrchen 0,1 ml einer Kaolin-Plättchenfaktor 3 - Mischung (Pathromtin (R) der Behringwerke AG, Marburg). Nach Mischung wird sechs min. bei 37°C inkubiert, anschließend jedes Röhrchen mit 0,1 ml einer 0,025 molaren Calciumchloridlösung versetzt und die Gerinnungszeiten bestimmt. Das Ergebnis zeigt Tabelle 1.

Figure imgb0001
Now 0.1 ml of a kaolin platelet factor 3 mixture (Pathromtin (R) from Behringwerke AG, Marburg) is added to each tube. After mixing, six minutes. Incubated at 37 ° C, then 0.1 ml of a 0.025 molar calcium chloride solution was added to each tube and the clotting times determined. The result is shown in Table 1.
Figure imgb0001

Aus den Gerinnungszeiten geht hervor, daß eine mit Normalplasma adsorbierte erfindungsgemäß hergestellte Kollagensuspension biologisch aktiven Gerinnungsfaktor VIII enthält.The coagulation times show that a collagen suspension prepared according to the invention and adsorbed with normal plasma contains biologically active coagulation factor VIII.

Beispiel 5:Example 5:

1 ml Kollagenlösung wird analog Beispiel 2 mit 1 ml Citrat-haltigem menschlichem Plasma beladen, die Kollagenfibrillen abzentrifugiert und dreimal mit Phosphatgepufferter physiologischer Kochsalzlösung gewaschen. Die Kollagenfibrillen werden mit für bestimmte Plasmaproteine spezifischen Antiseren vom Kaninchen im indirekten Fluoreszenztest auf adsorbierte Plasmaproteine untersucht. Mit Kaninchen-Normalserum wird eine negative, mit Anti-Humanfibrinogen, Anti-Human-Immunglobulin und Anti-Humanalbumin eine sehr schwache Reaktion gefunden. Mit Anti-Human-Faktor VIII-Serum wird eine sehr starke Reaktion gefunden.1 ml of collagen solution is loaded as in Example 2 with 1 ml of citrate-containing human plasma, the collagen fibrils are centrifuged off and washed three times with phosphate-buffered physiological saline. The collagen fibrils are examined with rabbit antisera specific for certain plasma proteins in an indirect fluorescence test for adsorbed plasma proteins. A negative reaction is found with normal rabbit serum and a very weak reaction with anti-human fibrinogen, anti-human immunoglobulin and anti-human albumin. A very strong reaction is found with anti-human factor VIII serum.

Dieses Beispiel zeigt die selektive und spezifische Bindung von Faktor VIII, der zum Beispiel gegenüber Albumin in 4.400-fach niedrigerer Konzentration im Plasma enthalten ist.This example shows the selective and specific binding of factor VIII, which is, for example, contained in the plasma at 4,400 times lower concentration than albumin.

Beispiel 6 :Example 6:

Beispiel 5 wird mit dem Plasma eines Patienten mit v.Willebrand'scher Krankheit ausgeführt, dessen Faktor VIII-Gehalt weniger als 10 % der Norm beträgt. Mit Antiserum gegen Faktor VIII wird nur eine schwache Reaktion beobachtet.Example 5 is carried out with the plasma of a patient with von Willbrand's disease, whose factor VIII content is less than 10% of the norm. A weak response is observed with factor VIII antiserum.

Beispiel 7 :Example 7:

Nach Beispiel 2 wird eine Adsorption von menschlichem Citratplasma mit steigenden Mengen von Kollagen durchgeführt. Die Plasmaüberstände werden auf ihren Gehalt an Faktor XIII untersucht. Der verwendete Test ist ein qualitatives Verfahren, das die Aktivitätsbereiche in % bezogen auf Normalplasma angibt. Unter Berücksichtigung der Ausgangsverdünnung von 1 : 2 werden die in Tabelle 2 angegebenen %-Werte gefunden.

Figure imgb0002
According to example 2, human citrate plasma is adsorbed with increasing amounts of collagen. The plasma supernatants are examined for their content of factor XIII. The test used is a qualitative procedure that gives the activity ranges in% based on normal plasma. Taking into account the initial dilution of 1: 2, the% values given in Table 2 are found.
Figure imgb0002

Beispiel 8 :Example 8:

In einem Aggregometer nach Born mit Schreiber (Fa.Braun, Melsungen, Bundesrepublik Deutschland) werden 1 ml blutplättchenreiches Citratplasma in die Küvette gefüllt. Photometer und Schreiber werden auf 0 % Transmission eingestellt. Es wird magnetisch gerührt und Temperaturangleich auf 370C abgewartet. Dann wird 1 µl der klaren Kollagenlösung nach Beispiel 1, entsprechend 1 µg Kollagen, mit einer Mikroliterspritze zugegeben. Innerhalb von zwei Minuten erfolgt eine Zusammenballung (Aggregation) der Blutplättchen zu großen Aggregaten, was zu einer starken Transmissionszunahme führt, welche von dem Schreiber aufgezeichnet wird. Diese Reaktion ist für die Diagnose von Gerinnungsstörungen geeignet.In a Born aggregator with scribe (Braun, Melsungen, Federal Republic of Germany), 1 ml of citrated plasma rich in platelets is filled into the cuvette. Photometer and recorder are set to 0% transmission. The mixture is stirred magnetically and the temperature is waited for to reach 37 ° C. Then 1 μl of the clear collagen solution according to Example 1, corresponding to 1 μg collagen, is added using a microliter syringe. The platelets aggregate into large aggregates within two minutes, which leads to a strong increase in transmission, which is recorded by the writer. This reaction is suitable for the diagnosis of coagulation disorders.

Beispiel 9 :Example 9:

Die Kollagenlösung wird auf etwa 35 bis 40°C erwärmt, so daß sie Fibrillen ausscheidet. Die gelartige Masse wird lyophilisiert, wodurch ein stabiles weißes Kollagenvlies erhalten wird. Der Kollagenlösung können Faktor VIII, Faktor XIII und/oder Fibrinogen zugesetzt worden sein.The collagen solution is heated to about 35 to 40 ° C so that it excretes fibrils. The gel-like mass is lyophilized, whereby a stable white collagen fleece is obtained. Factor VIII, Factor XIII and / or fibrinogen may have been added to the collagen solution.

Claims (7)

1. Verfahren zur Herstellung einer Kollagenlösung, dadurch gekennzeichnet, daß pepsinbehandeltes Kollagen gegen eine Phosphat-gepufferte isotonische Salzlösung dialysiert wird, die eine basische Aminosäure in einer Konzentration von 5 bis 20 nmol/1 enthält.1. A process for the preparation of a collagen solution, characterized in that pepsin-treated collagen is dialyzed against a phosphate-buffered isotonic saline solution which contains a basic amino acid in a concentration of 5 to 20 nmol / 1. 2. Eine Kollagenlösung erhältlich nach Anspruch 1, dadurch gekennzeichnet, daß sie beim Erwärmen auf eine Temperatur oberhalb Raumtemperatur Kollagenfibrillen ausscheidet.2. A collagen solution obtainable according to claim 1, characterized in that it secretes collagen fibrils when heated to a temperature above room temperature. 3. Verwendung einer Kollagenlösung nach Anspruch 2 zur Adsorption der Gerinnungsfaktoren VIII und XIII aus diese enthaltenden Flüssigkeiten.3. Use of a collagen solution according to claim 2 for the adsorption of coagulation factors VIII and XIII from liquids containing them. 4. Verwendung einer Kollagenflüssigkeit nach Anspruch 2 zur Herstellung von Kollagenfibrillen, an welche die Gerinnungsfaktoren VIII und XIII adsorbiert sind, und die gegebenenfalls Fibrinogen enthalten.4. Use of a collagen liquid according to claim 2 for the production of collagen fibrils to which the coagulation factors VIII and XIII are adsorbed and which may contain fibrinogen. 5. Verwendung einer Kollagenlösung nach Anspruch 2 als Diagnostikum.5. Use of a collagen solution according to claim 2 as a diagnostic. 6. Verwendung einer Kollagenlösung nach Anspruch 2 zur Herstellung eines Vlieses.6. Use of a collagen solution according to claim 2 for the production of a nonwoven. 7. Verwendung einer Kollagenlösung nach Anspruch 2 in einer kosmetischen Zubereitung.7. Use of a collagen solution according to claim 2 in a cosmetic preparation.
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Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0114351A2 (en) * 1982-12-27 1984-08-01 BEHRINGWERKE Aktiengesellschaft Process for the manufacture of a collagenous web
EP0114351B1 (en) * 1982-12-27 1989-07-26 BEHRINGWERKE Aktiengesellschaft Process for the manufacture of a collagenous web
EP0119076A2 (en) * 1983-03-10 1984-09-19 Koken Co. Ltd. A substrate comprising regenerated collagen fibrils
EP0119076A3 (en) * 1983-03-10 1986-07-23 Koken Co. Ltd. A substrate comprising regenerated collagen fibrils
FR2606412A1 (en) * 1986-11-06 1988-05-13 Merieux Inst FACTOR VIII PREPARATION PROCESS
EP0270413A1 (en) * 1986-11-06 1988-06-08 Institut Merieux Process for the preparation of factor VIII
EP0434354A1 (en) * 1989-12-21 1991-06-26 Kurita Water Industries Ltd. Separation material for blood coagulation factor, preparation and use thereof
US5096593A (en) * 1989-12-21 1992-03-17 Kurita Water Industries Ltd. Separation material derived from glucomannan for blood coagulation factor, preparation and use thereof
FR2680005A1 (en) * 1991-08-01 1993-02-05 Coletica Use of collagen as a solid substrate for fixing a sensor capable of reacting specifically with an element to be detected in a biological medium, reactant and implementation method
WO1993003373A1 (en) * 1991-08-01 1993-02-18 Coletica Use of collagen as a solid binding substrate for a specific sensor
US5648208A (en) * 1991-08-01 1997-07-15 Coletica Use of a collagen as solid binding substrate for a ligand capable of reacting specifically with an element to be detected in a biological medium, reactant and implementation
WO1998033820A1 (en) * 1997-02-04 1998-08-06 Baxter Aktiengesellschaft Method of chromatographically purifying or fractionating von willebrand factor from a vwf-containing starter material
US6414125B1 (en) 1997-02-04 2002-07-02 Baxter Aktiengesellschaft Method of chromatographically purifying or fractionating, respectively, von Willebrand factor from a VWF-containing starting material

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EP0023607A3 (en) 1981-04-15
US4404134A (en) 1983-09-13
US4331766A (en) 1982-05-25
ATE3866T1 (en) 1983-07-15
EP0023607B1 (en) 1983-06-22
DE3063883D1 (en) 1983-07-28
JPH0159280B2 (en) 1989-12-15
ZA804364B (en) 1981-07-29
JPS6461506A (en) 1989-03-08
ES8105011A1 (en) 1981-05-16
JPS5616403A (en) 1981-02-17
DE2929144A1 (en) 1981-02-12
IL60616A0 (en) 1980-09-16
CA1161756A (en) 1984-02-07
ES493359A0 (en) 1981-05-16
IL60616A (en) 1984-02-29

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